GUDIDData
emdn_classification Primary ID: W050101010202

BLOOD COLLECTION, TUBES WITHOUT ADDITIVES OR SERUM SEPARATOR (UDI W050101010202)

Manufactured by

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for BLOOD COLLECTION, TUBES WITHOUT ADDITIVES OR SERUM SEPARATOR - Primary ID W050101010202

Device Regulatory Overview

The BLOOD COLLECTION, TUBES WITHOUT ADDITIVES OR SERUM SEPARATOR (Model/Catalog Number: Unspecified) is a medical device manufactured by . This product is indexed under FDA Product Code / Category Classification W050101010202 within international Unique Device Identification (UDI) compliance databases.

ACTIVE SAFETY RECALL ALERT 3 Event(s) Found

Enforcement actions are currently active for this product line.

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Technical Specifications

Model Number
N/A
Product Code / EMDN
W050101010202
Device Name
BLOOD COLLECTION, TUBES WITHOUT ADDITIVES OR SERUM SEPARATOR
Database Sync Date
2026-08-09 16:18:37

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of BLOOD COLLECTION, TUBES WITHOUT ADDITIVES OR SERUM SEPARATOR?

The registered manufacturer of record for BLOOD COLLECTION, TUBES WITHOUT ADDITIVES OR SERUM SEPARATOR is .

What is the Primary UDI-DI identifier for BLOOD COLLECTION, TUBES WITHOUT ADDITIVES OR SERUM SEPARATOR?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is W050101010202.

What classification code is assigned to this device?

This device is registered under product classification code W050101010202.

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